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Silane, (2,5-thiophenediyldi-4,1-phenylene)bis[trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141775-93-1

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141775-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141775-93-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,7,7 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 141775-93:
(8*1)+(7*4)+(6*1)+(5*7)+(4*7)+(3*5)+(2*9)+(1*3)=141
141 % 10 = 1
So 141775-93-1 is a valid CAS Registry Number.

141775-93-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis(4-trimethylsilylphenyl)thiophene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:141775-93-1 SDS

141775-93-1Downstream Products

141775-93-1Relevant academic research and scientific papers

Synthesis of Thiophene/phenylene Co-oligomers. IV [1]. 6- to 8-Ring Molecules

Shu, Hotta,Katagiri, Toshifumi

, p. 845 - 850 (2007/10/03)

We report the synthesis of various thiophene/phenylene co-oligomers with total number of thiophene and benzene (phenylene) rings of 6 to 8. These compounds include a phenyl-capped sexithiophene, a thienyl-capped quaterphenylene, as well as block and alternating co-oligomers. The synthesis is based on either the Suzuki coupling reaction or the direct dimerization coupling. The latter method produces symmetric molecules with an even total ring number. These reaction schemes enables us to obtain the target compounds in high quality. Although the resulting materials are difficult to dissolve in organic solvents and therefore difficult to identify by usual 1H nmr spectroscopy, they have successfully been identified through Fourier-transform ir spectroscopy. The specific group frequencies of ring-stretching and out-of plane deformation modes are characteristic of the substitution pattern of the individual thiophene and benzene rings.

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